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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656407Generated: October 28, 2026

Borane → HCID 67173148, compound

https://huagongshe.com/reaction/656407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoraneHCID 6331—
ReactantHCID 67174106HCID 67174106—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67173148HCID 67173148—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of [(2S)-6-nitro-2′-oxo-1,1′,2′,3-tetrahydrospiro[indene-2,3′-pyrrolo[2,3-b]pyridin]-5-yl]acetic acid from Step D (753 mg, 2.22 mmol) in THF (15 mL), at −78° C., was added borane (1 M in THF; 9.1 mL, 9.1 mmol) dropwise. After 5 min, the mixture was warmed to 0° C. and stirring was continued at this temperature for 3 h. The reaction was quenched carefully with 1 N HCl and stirring was continued at ambient temperature. The mixture was adjusted to pH 8 with saturated aqueous NaHCO3 and extracted with EtOAc (2×100 mL). The combined organic layers were dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude product was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:MeOH—100:0 to 80:20, to give the title compound. MS: m/z=326 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071771B2
Source datasetuspto-grants-2011_12
ORD IDord-dbf413f73c124d4797b1475d29f265fe
Source noteuspto-grants-2011_12