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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708823Generated: November 1, 2026

Water → 2-[(1-{Bis[(tert-butoxy)carbonyl]amino}isoquinolin-6-yl)amino]-15,15-difluoro-4,17,20-trimethyl-3,12-dioxo-13-oxa-4,11-diazatricyclo[14.2.2.16,10]henicosa-1(18),6,8,10 (21),16,19-hexaene-7-carboxylic acid

https://huagongshe.com/reaction/708823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium HydroxideHCID 3939—
ReactantSodium BisulfateHCID 516919—
ReactantMethyl 2-[(1-{bis[(tert-butoxy)carbonyl]amino}isoquinolin-6-yl)amino]-15,15-difluoro-4,17,20-trimethyl-3,12-dioxo-13-oxa-4,11-diazatricyclo[14.2.2.16,10]henicosa-1(18),6,8,10 (21),16,19-hexaene-7-carboxylateHCID 118093104—
Solvent1,4-DioxaneHCID 31275—
Product2-[(1-{Bis[(tert-butoxy)carbonyl]amino}isoquinolin-6-yl)amino]-15,15-difluoro-4,17,20-trimethyl-3,12-dioxo-13-oxa-4,11-diazatricyclo[14.2.2.16,10]henicosa-1(18),6,8,10 (21),16,19-hexaene-7-carboxylic acidHCID 118098691100%

Reaction Steps

To a flask containing LiOH (38.7 mg, 1.617 mmol) was added water (8 mL). A solution of 4C (130 mg, 0.162 mmol) in dioxane (10 mL) was added and the reaction was stirred for 4.5 h. The reaction was partially evaporated to remove the dioxane then transferred to a funnel using H2O (3 mL) and EtOAc (3 mL). To the mixture was added 1N sodium bisulfate (3.23 mL, 3.23 mmol) followed by extraction with EtOAc (4×8 mL). The combined organics were dried (Na2SO4), filtered and concentrated to leave 4D (128 mg, 90% yield) as a white solid. About 10% of the material is mono-boc compound by LC/MS. 19F and MS are consistent with the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174974B2
Source datasetuspto-grants-2015_11
ORD IDord-598f262a4aef4aff92131a0ddbab536a
Source noteuspto-grants-2015_11