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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900101Generated: October 27, 2026

3-(Bromomethyl)-1H-indazole, N1-BOC protected → HCID 69314041, compound

https://huagongshe.com/reaction/900101

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Bromomethyl)-1H-indazole, N1-BOC protectedHCID 10804951—
ReactantN-isopropyl-2-(5-oxo-1-phenyl-4,5-dihydro-2,3,6,10b-tetraaza-benzo[e]azulen-6-yl)-N-phenyl-acetamideHCID 58957944—
ProductHCID 69314041HCID 6931404163%

Reaction Steps

Following the procedure described for Example 3(A), Step A, N-isopropyl-2-(5-oxo-1-phenyl-4,5-dihydro-2,3,6,10b-tetraaza-benzo[e]azulen-6-yl)-N-phenyl-acetamide (Preparation 7(A)) (411.7 mg, 0.9118 mmol) was alkylated with 3-bromomethyl-indazole-1-carboxylic acid tert-butyl ester (309 mg, 0.993 mmol). Purification by medium pressure chromatography eluting with a solvent gradient (EtOAc to 5% MeOH in EtOAc) provided 391.9 mg of 3-{6-[(isopropyl-phenyl-carbamoyl)-methyl]-5-oxo-1-phenyl-5,6-dihydro-4H-2,3,6,10b-tetraaza-benzo[e]azulen-4-ylmethyl}-indazole-1-carboxylic acid tert-butyl ester. 1H NMR (CD3OD) δ 7.99 (m, 2H), 7.22-7.66 (m, 15H), 7.01 (dd, 1H), 4.53-4.81 (m, 3H), 3.88-4.21 (m, 3H), 1.65 (m, 9H), 0.94 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07358242B2
Source datasetuspto-grants-2008_04
ORD IDord-4011ebaceaba46f38057409828678727
Source noteuspto-grants-2008_04