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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972892Generated: November 2, 2026

Methanesulfonic Acid → HCID 58529408, compound

https://huagongshe.com/reaction/1972892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantHCID 58529969HCID 58529969—
SolventDichloromethaneHCID 6344—
ProductHCID 58529408HCID 58529408617.8%

Reaction Steps

[4-Amino-5-(2-benzyl-2H-indazol-6-yl)-pyrrolo[2,1-f][1,2,4]triazin-7-yl]-(1,2,3,4-tetrahydro-isoquinolin-7-yl)-methanone (0.050 g, 0.01 mmol) was dissolved in dichloromethane (1 mL) and methanesulfonic acid (0.104 mL, 1.61 mmol) was added followed by Et3SIH (0.128 mL, 0.80 mmol). The resulting mixture was stirred at rt overnight. The mixture was diluted with dichloromethane and washed with saturated aqueous NaHCO3, water and brine. The organic layer was concentrated, suspended in MeOH and filtered to give a desired product as white solid (30 mg, 62%). 1H-NMR (CD3OD-d4) 8.28-8.24 (m, 1 H), 7.78 (s, 1 H), 7.70 (dd, 1H), 7.59-7.56 (m, 1 H), 7.33-7.23 (m, 5 H), 7.11 (dd, 1 H), 7.07-6.89 (m, 3 H), 6.39 (s, 1 H), 5.57 (s, 2 H), 4.16 (s, 2 H), 3.82 (s, 2 H), 2.96 (t, 2 H), 2.71 (t, 2 H); LC-MS [M+H]+=486.3, RT=2.30 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431695B2
Source datasetuspto-grants-2013_04
ORD IDord-d6cc11e3a0214fa0b9fe615b04304a77
Source noteuspto-grants-2013_04